abnormal iris pigment epithelium_Foxc2<tm1Blh>/Foxc2<+>

http://metadb.riken.jp/0005199I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2Foxc2Foxc2tm1Blh

abnormal iris pigment epithelium_Foxc2<tm1Blh>/Foxc2<+>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• forkhead box C2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347481

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Foxc2<tm1Blh>/Foxc2<+>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Foxc2<+>|Foxc2<tm1Blh>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• involves: 129S6/SvEvTac * Black Swiss

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• abnormal iris pigment epithelium
  http://purl.obolibrary.org/obo/MP_0005199

文献

http://purl.org/net/cito/citesAsAuthority

• R S. Smith, et.al., Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development., Human molecular genetics, 2000, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/10767326